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Summary Literature (0)
DOID:0050760 - X-linked myopathy with excessive autophagy

Disease Ontology Definition:A myopathy that is characterized by childhood onset of progressive muscle weakness and atrophy primarily affecting the proximal muscles in males between 5 and 10 years old, has_material_basis_in mutation in the VMA21 gene on chromosome Xq28.

Synonyms: XMEA

Xenbase Genes : vma21

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010684 - X-linked myopathy with excessive autophagy


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): myopathy (is_a)